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FDA 510(k)

SURGICAL RETRACTOR/BLUNT DISSECTOR

K-Number: K933009 · 1993-09-03

ApplicantAdvanced Surgical, Inc.
Decision Date1993-09-03
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGICAL RETRACTOR/BLUNT DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical, Inc.. It received FDA 510(k) clearance on 1993-09-03 under 510(k) number K933009. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL RETRACTOR/BLUNT DISSECTOR?

SURGICAL RETRACTOR/BLUNT DISSECTOR is a medical device that received FDA 510(k) clearance on 1993-09-03. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K933009.

When did SURGICAL RETRACTOR/BLUNT DISSECTOR receive FDA 510(k) clearance?

SURGICAL RETRACTOR/BLUNT DISSECTOR received FDA 510(k) clearance on 1993-09-03, under 510(k) number K933009.

Who is the listed applicant for SURGICAL RETRACTOR/BLUNT DISSECTOR?

The FDA 510(k) record lists Advanced Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL RETRACTOR/BLUNT DISSECTOR?

The FDA product code for SURGICAL RETRACTOR/BLUNT DISSECTOR is GCJ.

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Related Devices (Code: GCJ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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